Detalhe da pesquisa
1.
Jansen-de Vries syndrome: Expansion of the PPM1D clinical and phenotypic spectrum in 34 families.
Am J Med Genet A
; 191(7): 1900-1910, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37183572
2.
An Open-Label Study of Cranial Electrotherapy Stimulation on Behavioral Regulation in a Mixed Neurodevelopmental Clinical Cohort.
J Integr Neurosci
; 22(5): 119, 2023 Aug 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37735126
3.
Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental Disorders.
Am J Hum Genet
; 105(3): 631-639, 2019 09 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31353024
4.
Pathogenic MAST3 Variants in the STK Domain Are Associated with Epilepsy.
Ann Neurol
; 90(2): 274-284, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34185323
5.
Heteromeric Assembly of Truncated Neuronal Kv7 Channels: Implications for Neurologic Disease and Pharmacotherapy.
Mol Pharmacol
; 98(3): 192-202, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32580997
6.
De Novo Truncating Mutations in the Last and Penultimate Exons of PPM1D Cause an Intellectual Disability Syndrome.
Am J Hum Genet
; 100(4): 650-658, 2017 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28343630
7.
De novo and biallelic DEAF1 variants cause a phenotypic spectrum.
Genet Med
; 21(9): 2059-2069, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30923367
8.
The Contribution of the Corpus Callosum to Language Lateralization.
J Neurosci
; 36(16): 4522-33, 2016 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-27098695
9.
Chronic stress is associated with reduced circulating hematopoietic progenitor cell number: A maternal caregiving model.
Brain Behav Immun
; 59: 245-252, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27622676
10.
Reciprocal white matter alterations due to 16p11.2 chromosomal deletions versus duplications.
Hum Brain Mapp
; 37(8): 2833-48, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27219475
11.
16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.
Am J Med Genet A
; 170(11): 2943-2955, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27410714
12.
Aberrant white matter microstructure in children with 16p11.2 deletions.
J Neurosci
; 34(18): 6214-23, 2014 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-24790192
13.
Shared and Divergent Auditory and Tactile Processing in Children with Autism and Children with Sensory Processing Dysfunction Relative to Typically Developing Peers.
J Int Neuropsychol Soc
; 21(6): 444-54, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26145730
14.
Autism traits in the RASopathies.
J Med Genet
; 51(1): 10-20, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24101678
15.
White matter microstructure of children with sensory over-responsivity is associated with affective behavior.
J Neurodev Disord
; 16(1): 1, 2024 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38166648
16.
Global MEG Resting State Functional Connectivity in Children with Autism and Sensory Processing Dysfunction.
bioRxiv
; 2024 Jan 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38352614
17.
Quantifying attention span across the lifespan.
Front Cognit
; 22023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37920687
18.
Hemispheric lateralization of white matter microstructure in children and its potential role in sensory processing dysfunction.
Front Neurosci
; 17: 1088052, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37139524
19.
Neurite orientation dispersion and density imaging of white matter microstructure in sensory processing dysfunction with versus without comorbid ADHD.
Front Neurosci
; 17: 1136424, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37492404
20.
Examining the Latent Structure and Correlates of Sensory Reactivity in Autism: A Multi-site Integrative Data Analysis by the Autism Sensory Research Consortium.
Res Sq
; 2023 Jan 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36712092